1. Academic Validation
  2. In vitro and in vivo antibacterial activities of KB-5246, a new tetracyclic quinolone

In vitro and in vivo antibacterial activities of KB-5246, a new tetracyclic quinolone

  • Antimicrob Agents Chemother. 1989 Nov;33(11):1896-900. doi: 10.1128/AAC.33.11.1896.
Y Kotera 1 S Mitsuhashi
Affiliations

Affiliation

  • 1 Episome Institute, Gunma-ken, Japan.
Abstract

The in vitro and in vivo Antibacterial activities of KB-5246, a tetracyclic Quinolone, were compared with those of ciprofloxacin, ofloxacin, and norfloxacin. KB-5246 demonstrated a broad Antibacterial spectrum. The in vitro activity of KB-5246 against gram-negative bacteria was higher than that of ofloxacin or norfloxacin and was comparable to that of ciprofloxacin. KB-5246 demonstrated the greatest activity against gram-positive bacteria of the four agents tested. Among Streptococcus pyogenes strains resistant to 1.56 micrograms of norfloxacin per ml, there were 26 strains susceptible to 0.2 micrograms of KB-5246 per ml. Similarly, among the Staphylococcus aureus and Staphylococcus epidermidis strains resistant to 3.13 micrograms of norfloxacin per ml, there were 23 S. aureus and 11 S. epidermidis strains susceptible to 0.39 micrograms of KB-5246 per ml. Among the Streptococcus pneumoniae and Enterococcus faecalis strains resistant to 12.5 micrograms of norfloxacin per ml, there were 5 S. pneumoniae and 10 E. faecalis strains susceptible to 0.39 micrograms of KB-5246 per ml. KB-5246 had bactericidal activity at the MIC. KB-5246 demonstrated excellent Antibacterial activity against various systemic infections in mice. After oral administration, KB-5246 was as active as ofloxacin and about two times more active than norfloxacin.

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